Assessment of hepatic prostaglandin E2 level in carbamazepine induced liver injury

Objective. Carbamazepine (CBZ), a widely used antiepileptic drug, is one major cause of the idiosyncratic liver injury along with immune reactions. Conversely, prostaglandin E₂ (PGE2) demonstrates a hepatoprotective effect by regulating immune reactions and promoting liver repair in various types of liver injury. However, the amount of hepatic PGE₂ during CBZ-induced liver injury remains elusive. In this study, we aimed to evaluate the hepatic PGE₂ levels during CBZ-induced liver injury using a mouse model.

Methods. Mice were orally administered with CBZ at a dose of 400 mg/kg for 4 days, and 800 mg/kg on the 5th day.

Results. Plasma alanine transaminase (ALT) level increased in some of mice 24 h after the last CBZ administration. Although median value of hepatic PGE₂ amount in the CBZ-treated mice showed same extent as vehicle-treated control mice, it exhibited significant elevated level in mice with severe liver injury presented by a plasma ALT level >1000 IU/L. According to these results, mice had a plasma ALT level >1000 IU/L were defined as responders and the others as non-responders in this study. Even though, the hepatic PGE₂ levels increased in responders, the hepatic expression and enzyme activity related to PGE₂ production were not upregulated when compared with vehicle-treated control mice. However, the hepatic 15-hydroxyprostaglandin dehydrogenase (15-PGDH) expression and activity decreased significantly in responders when compared with control mice.

Conclusions. These results indicate that elevated hepatic PGE₂ levels can be attributed to the downregulation of 15-PGDH expression under CBZ-induced liver injury.